APOA5, apolipoprotein A5, 116519

N. diseases: 107; N. variants: 22
Disease: Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C3489395
Disease: Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial
Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 0.500 None 1.000 2 2015 2018